Access the full text.
Sign up today, get DeepDyve free for 14 days.
Antonio Ramirez, E. Lobkovsky, D. Collum (2003)
Hemilabile ligands in organolithium chemistry: substituent effects on lithium ion chelation.Journal of the American Chemical Society, 125 50
N. Jung, S. Bräse (2012)
New catalysts for the transition-metal-catalyzed synthesis of aziridines.Angewandte Chemie, 51 23
B. Bucholz, H. Stamm (1986)
Reactions with Aziridines, XXXII[1]. Mechanistic Aspects in Nucleophilic Opening of Three‐Membered Rings. Alcoholyses of Activated AziridinesIsrael Journal of Chemistry, 27
P. Kuijpers, J. Vlugt, S. Schneider, B. Bruin (2017)
Nitrene Radical Intermediates in Catalytic SynthesisChemistry (Weinheim an Der Bergstrasse, Germany), 23
M. Torres, B. Cassels, M. Rezende (1995)
The Preparation of Potentially Psychoactive β-AlkoxyphenethylaminesSynthetic Communications, 25
T. Katsuki* (2005)
Azide Compounds: Nitrogen Sources for Atom-efficient and Ecologically Benign Nitrogen-atom-transfer ReactionsChemistry Letters, 34
Christian Stanetty, M. Blaukopf, B. Lachmann, C. Noe (2011)
The Dinosyl Group: A Powerful Activator for the Regioselective Alcoholysis of AziridinesEuropean Journal of Organic Chemistry, 2011
Kurtis Carsch, Ida DiMucci, D. Iovan, Alex Li, Shao-Liang Zheng, C. Titus, Sang Lee, K. Irwin, D. Nordlund, K. Lancaster, T. Betley (2019)
Synthesis of a copper-supported triplet nitrene complex pertinent to copper-catalyzed aminationScience, 365
M. Ghorai, Yerramsetti Nanaji (2013)
Synthetic route to chiral indolines via ring-opening/C-N cyclization of activated 2-haloarylaziridines.The Journal of organic chemistry, 78 8
P. Lu (2010)
Recent Developments in Regioselective Ring Opening of AziridinesChemInform, 41
H. Guyon, A. Boussonnière, Anne‐Sophie Castanet (2017)
Readily Accessible 1,2-Amino Ether Ligands for Enantioselective Intramolecular Carbolithiation.The Journal of organic chemistry, 82 9
R. Sott, J. Granander, G. Hilmersson (2004)
Mixed complexes formed by lithioacetonitrile and chiral lithium amides: observation of (6)li,(15)N and (6)Li,(13)C couplings due to both C-Li and N-Li contacts.Journal of the American Chemical Society, 126 21
Jiawei Liu, Chuan Wang (2020)
Zinc-Catalyzed Hydroxyl-Directed Regioselective Ring Opening of Aziridines in SN2 Reaction PathwayACS Catalysis, 10
J. Llaveria, Álvaro Beltrán, W. Sameera, Abel Locati, M. Díaz‐Requejo, M. Matheu, S. Castillón, F. Maseras, P. Pérez (2014)
Chemo-, regio-, and stereoselective silver-catalyzed aziridination of dienes: scope, mechanistic studies, and ring-opening reactions.Journal of the American Chemical Society, 136 14
Susann Krake, S. Bergmeier (2010)
Inter- and intramolecular reactions of epoxides and aziridines with π-nucleophilesTetrahedron, 66
P. Müller, Corinne Fruit (2003)
Enantioselective catalytic aziridinations and asymmetric nitrene insertions into CH bonds.Chemical reviews, 103 8
W. McCoull, F. Davis (2000)
Recent Synthetic Applications of Chiral AziridinesSynthesis, 2000
Xiaofei Fu, Wenxian Zhao (2019)
Progress in Difunctionalization of AlkenesChinese Journal of Organic Chemistry
L. Degennaro, Piera Trinchera, R. Luisi (2014)
Recent advances in the stereoselective synthesis of aziridines.Chemical reviews, 114 16
Yingguang Zhu, Qian Wang, Richard Cornwall, Yian Shi (2014)
Organocatalytic asymmetric epoxidation and aziridination of olefins and their synthetic applications.Chemical reviews, 114 16
C. Franchini, A. Carocci, A. Catalano, M. Cavalluzzi, F. Corbo, G. Lentini, A. Scilimati, P. Tortorella, D. Camerino, A. Luca (2003)
Optically active mexiletine analogues as stereoselective blockers of voltage-gated Na(+) channels.Journal of medicinal chemistry, 46 24
Hongnan Sun, C. Yang, Run Lin, W. Xia (2014)
Regioselective Ring-Opening Nucleophilic Addition of Aziridines through Photoredox CatalystAdvanced Synthesis & Catalysis, 356
Satoru Teranishi, Kazuki Maeda, T. Kurahashi, S. Matsubara (2019)
Diastereoselective Synthesis of 1,3-Oxazolidines via Cationic Iron Porphyrin-catalyzed Cycloaddition of Aziridines with Aldehydes.Organic letters, 21 8
Fabian Dielmann, D. Andrada, G. Frenking, G. Bertrand (2014)
Isolation of bridging and terminal coinage metal-nitrene complexes.Journal of the American Chemical Society, 136 10
Mauricio Osorio-Olivares, M. Rezende, S. Sepúlveda-Boza, B. Cassels, A. Fierro (2004)
MAO inhibition by arylisopropylamines: the effect of oxygen substituents at the beta-position.Bioorganic & medicinal chemistry, 12 15
I. Watson, Lily Yu, A. Yudin (2006)
Advances in nitrogen transfer reactions involving aziridines.Accounts of chemical research, 39 3
Melinda Nonn, A. Remete, F. Fülöp, L. Kiss (2017)
Recent advances in the transformations of cycloalkane-fused oxiranes and aziridinesTetrahedron, 73
J. Kalow, A. Doyle (2013)
Enantioselective fluoride ring opening of aziridines enabled by cooperative Lewis acid catalysisTetrahedron, 69
Luca Legnani, B. Morandi (2016)
Direct Catalytic Synthesis of Unprotected 2-Amino-1-Phenylethanols from Alkenes by Using Iron(II) Phthalocyanine.Angewandte Chemie, 55 6
Oriol Salvadó, Riccardo Gava, E. Fernández (2019)
Diborylalkyllithium Salts Trigger Regioselective Ring Opening of Vinyl Aziridines.Organic letters
Yizhou Zhao, Gang‐Wei Wang, Shanshan Zhou, Zhong-Jun Li, Xiangbao Meng (2014)
Diastereoselective formation of aziridines from diazocarbonyl compounds and N-(O-pivaloylated D-galactosyl)benzylideneamines and ring-opening reactions with p-toluenethiol.Organic & biomolecular chemistry, 12 21
C. Thibodeaux, Wei‐chen Chang, Hung‐wen Liu (2012)
Enzymatic chemistry of cyclopropane, epoxide, and aziridine biosynthesis.Chemical reviews, 112 3
X. Hu (2004)
Nucleophilic ring opening of aziridinesTetrahedron, 60
Daichi Kawauchi, H. Ueda, H. Tokuyama (2019)
Double Functionalization of Styrenes by Cu-Mediated Assisted Tandem CatalysisEuropean Journal of Organic Chemistry
K. O’Brien, F. Kelleher (2013)
Synthesis of Orthogonally Protected 1,2-diaminopropanoic Acids by Ring-Opening of 3-Unsubstituted N-Activated Aziridine 2-Carboxylates with Para-Methoxybenzylamine: a Study of the Regioselectivity of the ReactionTetrahedron Letters, 54
D. Tanner (1994)
Chiral Aziridines—Their Synthesis and Use in Stereoselective TransformationsAngewandte Chemie, 33
P. Dauban, R. Dodd (2003)
Iminoiodanes and C-NBond Formation in Organic SynthesisSynlett, 2003
J. Llaveria, A. Espinoza, G. Negrón, M. Matheu, S. Castillón (2012)
Efficient and regioselective ring-opening of arylaziridines with alcohols, thiols, amines and N-heteroaromatic compounds using sulphated zirconiaTetrahedron Letters, 53
Jennifer Ciesielski, Geoffroy Dequirez, P. Retailleau, V. Gandon, P. Dauban (2016)
Rhodium-Catalyzed Alkene Difunctionalization with Nitrenes.Chemistry, 22 27
Yosra Badiei, Adriana Dinescu, X. Dai, R. Palomino, F. Heinemann, T. Cundari, T. Warren (2008)
Copper-nitrene complexes in catalytic C-H amination.Angewandte Chemie, 47 51
A copper‐catalyzed three‐component tandem reaction of alkenes, sulfonyl azides, and alcohols is described. This straightforward transformation provides a practical method for the synthesis of valuable β‐alkoxy amines from easily accessible starting materials under comparative cheap copper catalysis without external ligands though regioselective ring‐opening reaction of aziridine intermediates. This reaction has a broad functional groups tolerance and the yields are generally good.
Asian Journal of Organic Chemistry – Wiley
Published: May 1, 2021
Keywords: ; ; ; ;
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.